Allele Registry

Canonical Allele Identifier: PA2825168715

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000723641

RCV001081479

RCV004537312

ClinVar Variation:

92981

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Phe2371Val	CA220795 NM_000426.4:c.7111T>G